Kim Seong Ho, Yasunaga Adam B, Zhang Hongyuan, Whitley Kevin D, Li Isaac T S
Department of Chemistry, University of British Columbia, Kelowna, BC, V1V 1V7, Canada.
Department of Chemistry and Advanced Materials, College of Natural Sciences, Gangneung-Wonju National University, Gangneung, 25457, Republic of Korea.
Adv Sci (Weinh). 2025 Jul;12(28):e2408280. doi: 10.1002/advs.202408280. Epub 2025 Apr 17.
DNA-based molecular tension probes have revolutionized the localization of mechanical events in live cells with super-resolution. However, imaging the magnitude of these forces at super-resolution has been challenging. Here, qtPAINT (quantitative tension points accumulation for imaging in nanoscale topography) is introduced as a strategy to image the magnitude of molecular tension with super-resolution accuracy. By leveraging the force-dependent dissociation kinetics of short DNA oligonucleotides on their complementary strands, tension is encoded on individual molecules through their binding kinetics. This method allowed for a quantitative analysis of these kinetics, providing a detailed reconstruction of the force magnitudes acting on each tension probe. The technique integrates a molecular-beacon PAINT imager with a hairpin molecular tension probe, achieving a force quantification range of 9-30 pN and maintaining a spatial resolution of 30-120 nm in low and high-density regions. Additionally, qtPAINT offers a temporal resolution on the order of a minute, enhancing its applicability for studying dynamic cellular processes.
基于DNA的分子张力探针通过超分辨率技术彻底改变了活细胞中机械事件的定位。然而,以超分辨率成像这些力的大小一直具有挑战性。在这里,qtPAINT(用于纳米级形貌成像的定量张力点积累)作为一种以超分辨率精度成像分子张力大小的策略被引入。通过利用短DNA寡核苷酸与其互补链上的力依赖性解离动力学,张力通过其结合动力学编码在单个分子上。该方法允许对这些动力学进行定量分析,提供作用于每个张力探针的力大小的详细重建。该技术将分子信标PAINT成像仪与发夹分子张力探针相结合,在低密度和高密度区域实现了9-30 pN的力定量范围,并保持了30-120 nm的空间分辨率。此外,qtPAINT提供了大约一分钟的时间分辨率,增强了其在研究动态细胞过程中的适用性。